x-linked myopathy with excessive autophagy Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

10 genes co-occuring with the disease x-linked myopathy with excessive autophagy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
LAMP2 lysosomal-associated membrane protein 2 1.81239
GAA glucosidase, alpha; acid 1.20569
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase 0.792131
ATP12A ATPase, H+/K+ transporting, nongastric, alpha polypeptide 0.75412
ATP4A ATPase, H+/K+ exchanging, alpha polypeptide 0.75412
EMD emerin 0.698313
LAMA2 laminin, alpha 2 0.61866
DMD dystrophin 0.191719
HLA-A major histocompatibility complex, class I, A 0.17896
ACHE acetylcholinesterase (Yt blood group) 0.177029